A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124105



Internal ID19278344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:96208219..96208272hg38UCSC Ensembl
Outerchr6:96656095..96656148hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958174, nssv3975819
SamplesKWS2, KWS1
Known GenesFUT9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124105
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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